HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 352072Erstellt: 24. Oktober 2026
Toluene → 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole
https://huagongshe.com/de/reaction/352072
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 1,3-Dichloroacetone | HCID 10793 | — |
| Edukt | 4-(Trifluoromethyl)cinnamamide | HCID 5709014 | — |
| Edukt | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole | HCID 12992846 | 65% |
Reaktionsschritte
(E)-3-(4-(Trifluoromethyl)phenyl)-2-propenamide (10.0 g,46.5 mmol) and 1,3-dichloroacetone (11.0 g, 86.6 mmol) were added to toluene (50 ml), and the mixture was subjected to refluxing azeotropic dehydration using a Dean-Stark tube for 8.5 hours. The reaction mixture was concentrated under reduced pressure. To the residue were added dimethyl sulfoxide (50 ml) and sodium acetate trihydrate (15.8 g, 116.1 mmol). The mixture was stirred at 70-75° C. for 4 hours. Methanol (50 ml) was added. After allowing-to cool to room temperature and stirring; the mixture was stirred under ice-cooling for 1 hour. The precipitated crystals were collected by filtration, washed with cold-methanol (30 ml) and dried under reduced pressure to give 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole (13.1 g, yield 65%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06743924B2 |
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| Quelldatensatz | uspto-grants-2004_06 |
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| ORD ID | ord-6c7a09e552c3430f98ac75e781c5f0fa |
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| Quellennotiz | uspto-grants-2004_06 |
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